Canonical Allele Identifier: CA355472518

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704785C>T (hg19) ; chr3:g.180986997C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986997C>T , CM000665.2:g.180986997C>T	GRCh38
NC_000003.11:g.180704785C>T , CM000665.1:g.180704785C>T	GRCh37
NC_000003.10:g.182187479C>T	NCBI36
NG_022933.1:g.7778G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.226G>A
ENST00000482363.2:n.1322G>A
ENST00000485675.2:n.1316G>A
ENST00000688055.1:c.155G>A	ENSP00000508688.1:p.Gly52Asp
ENST00000382564.8:c.155G>A MANE Select	ENSP00000372005.2:p.Gly52Asp
ENST00000643241.1:c.80G>A	ENSP00000496401.1:p.Gly27Asp
ENST00000646965.1:c.-46-1001G>A	ENSP00000496456.1:n.-46-1001G>A
ENST00000382564.6:c.155G>A	ENSP00000372005.2:p.Gly52Asp
ENST00000469657.5:c.130-1001G>A	ENSP00000418058.1:n.130-1001G>A
ENST00000478723.5:n.294G>A
ENST00000479269.5:c.80G>A	ENSP00000419191.1:p.Gly27Asp
ENST00000485675.1:n.1228G>A
ENST00000486355.1:c.154+1G>A	ENSP00000419991.1:n.154+1G>A
ENST00000491873.5:c.80G>A	ENSP00000420767.1:p.Gly27Asp
NM_001190233.1:c.80G>A	NP_001177162.1:p.Gly27Asp
NM_145261.3:c.155G>A	NP_660304.1:p.Gly52Asp
NR_033721.1:n.275G>A
NR_033722.1:n.302-1001G>A
NR_033723.1:n.326+1G>A
NR_046073.1:n.176-1001G>A
NM_145261.4:c.155G>A MANE Select	NP_660304.1:p.Gly52Asp
NM_001190233.2:c.80G>A	NP_001177162.1:p.Gly27Asp
NR_033721.2:n.237G>A
NR_033722.2:n.264-1001G>A